@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_head
{
this:
np:hasAssertion
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_assertion
;
np:hasProvenance
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_provenance
;
np:hasPublicationInfo
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_assertion
a
np:Assertion
.
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_provenance
a
np:Provenance
.
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_assertion
{
miriam-gene:6311
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNfe3d6fba0799e623de7b4346948ad515
sio:SIO_000628
miriam-gene:6311
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_provenance
{
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_assertion
dcterms:description
"[In conclusion, our findings confirm the role of ATXN2 as an important risk factor for ALS and support the hypothesis that expanded ATXN2 repeats may predispose to other neurodegenerative diseases, including progressive supranuclear palsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:21610160
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP538178.RAmnNcaZWLaQhSTi5c3kAj_7U6trWNmZW76uq109kZKRY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}